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| Deafness_Isolated v1.76 | MAP3K1 | Zornitza Stark Marked gene: MAP3K1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.76 | MAP3K1 | Zornitza Stark Gene: map3k1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v1.76 | MAP3K1 |
Zornitza Stark gene: MAP3K1 was added gene: MAP3K1 was added to Deafness_Isolated. Sources: Literature Mode of inheritance for gene: MAP3K1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MAP3K1 were set to 39062623 Phenotypes for gene: MAP3K1 were set to Hearing loss disorder, MONDO:0005365, MAP3K1-related Review for gene: MAP3K1 was set to RED Added comment: Single family reported with homozygous missense variant but two supportive mouse models. Sources: Literature |
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